Sustainable ZIF‐67/Mo‐MXene‐Derived Nanoarchitecture Synthesis: An Enhanced Durable Performance of Lithium–Selenium Batteries

Selenium-based electrodes have garnered attention for their high electrical conductivity, compatibility with carbonate electrolytes, and volumetric capacity comparable to sulfur electrodes. However, real-time application is hindered by rapid capacity deterioration from the "shuttle effect" of polyselenides and volume fluctuations. To address these challenges, a hybrid Se@ZIF-67/Mo-MXene-derived (Se@Co-NC/Mo₂C) nanoarchitecture is developed via an economically viable in situ electrostatic self-assembly of ZIF-67 and Mo₂C nanosheets. The catalytic effects and porous framework of Co-NC/Mo₂C enhance electrode attributes, promoting superior adsorption and conversion of lithium polyselenides and facile ion/electron transport within the electrode, resulting in stable electrochemical performance. Lithium-selenium batteries (LSeBs) exhibit remarkable characteristics, boasting high specific capacity and exceptional durability. The Se@Co-NC/Mo₂C electrode delivers a reversible capacity of 503.5 mAh g^-1 at 0.5 C with 98% capacity retention, 100% Coulombic efficiency, and exceptional cyclic durability through 8600 cycles. In sustainability tests at 10C/1C charging/discharging, the Se@Co-NC/Mo₂C electrode demonstrates an optimistic and stable capacity of ≈370.6 mAh g^-1 with 93% capacity retention at the 3100^th cycle in a carbonate-based electrolyte and ≈181.3 mAh g^-1 with 92% capacity retention after 5000 cycles in an ether-based electrolyte, indicating exceptional stability for practical rechargeable batteries. This cost-effective and efficient approach holds significant potential for high-performance and durable LSeBs.